| Título: | Increased Prevalence 12308 A > G mutation in Mitochondrial tRNALeu (CUN) Gene Associated with earlier Age of Onset in Friedreich Ataxia |
| Autores: |
HEIDARI, Mohammad Medhi; PhD, assistant Professor of Molecular Genetics, Department of Biology,Sciences School,Yazd University of Medical Sciences, Yazd,Iran KHATAMI, Mehri; PhD, assistant Professor of Molecular Genetics, Department of Biology,Sciences School,Yazd University of Medical Sciences, Yazd,Iran HOUSHMAND, Massoud; PhD, Assistant professor of Human Molecular Genetics,Department of Medical Genetic,National Institute of Genetic Engineering and Biotechnology,Tehran,Iran MAHMOUDI, Eisa; PhD, assitant Professor of Mathematical Statistic,Department of Statistics,Yazd University, Yazd,Iran NAFISSI, Shahriar; MD, Associate Professor of Neurology, Neurology Department, Tehran University of Medical Sciences, Tehran,Iran |
| Fecha: | 2011-11-28 |
| Publicador: | Iranian Journal of Child Neurology |
| Fuente: |
 |
| Tipo: |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion original articles |
| Tema: | Friedreich ataxia; tRNALeu (CUN) gene; mitochondrial DNA; Mutation; TTGE |
| Descripción: | How to Cite this Article: Heidari MM, Khatami M, Houshmand M, Mahmoudi E, Nafissi Sh .Increased Prevalence 12308 A > G mutation in MitochondrialtRNALeu (CUN) Gene Associated with earlier Age of Onset in Friedreich Ataxia. Iranian Journal of Child Neurology 2011;5(4):25-31.Objective Friedreich ataxia (FRDA) is an inherited recessive disorder. Mitochondrial DNA is a candidate modifying factor for FRDA.The purpose of this study was to investigate the relationship between the tRNALeu (CUN) 12308 A> G mutation and age of onset in Friedreich ataxia.Materials & Methods The 12308 A> G substitution in mitochondrial tRNALeu (CUN) was examined in DNA samples from 30 Friedreich ataxia patients and 48 control subjects by temporal temperature gradient gel electrophoresis (TTGE) and sequencing. Logistic regression was used to determine of cutoff age of onset.ResultsTwenty-two patients had the 12308 A> G mutation, and we found that its overall prevalence was significantly higher in 20 patients aged 17 years or younger than in 2 patients aged over 17 years (90% versus 10%). The 12308 A> G mutation lies in a region that has been highly conserved between species.Conclusion Our results show that the 12308 A > G mutation is associated with earlier age of onset in Friedreich ataxia. Thus, this mutation might cause the younger age of onset in FRDA.References Grabczyk E, Usdin K. The GAA*TTC triplet repeat expanded in Friedreich ataxia impedes transcription elongation by T7 RNA polymerase in a length and supercoil dependent manner. Nucleic Acids Res 2000;28(14):2815-22.Sakamoto N, Chastain PD, Parniewski P, Ohshima K, Pandolfo M, Griffith JD, et al. Sticky DNA: self association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich ataxia. 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| Idioma: | Inglés |
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